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LIVER TOMOURS
DR.SYED UBAID
M.S(KEM MUMBAI)
FMAS
LAPAROSCOPIC AND GENERAL
SURGEON
ASSOCIATE PROFESSOR OF
SURGERY IIMSR,JALNA
WORKUP ALGORYHM FOR LIVER MASS
Mass on scan
History of prior
malignancy
No history of prior
malignancy
History
• Symptoms - abdominal pain/ pressure
effect,fever,anoraxia,weight loss
• Patient characteristics (age, gender, use
of OCP, risk factors for chronic liver
disease )
• History or findings of extrahepatic
malignancy
Physical examination and investigation
• Sign of chronic liver stigmata or portal
hypertention
• Lymphadenopathy
• CBC with PLT , coagulogram , LFT , hepatitis
profile , tumor marker
• Ultrasound , CT scan , MRI
Find needle biopsy
• commonly used to assist in the diagnosis of a
variety of liver lesions
• Disadventage
– Increase risk of bleeding and seeding of neoplastic
cells
– Some type liver lesion cannot diagnosis such as
hepatic adenomas and focal nodular hyperplasia
Multiphasic CT
For detection of liver lesions
• Non enhance CT
• Arterial phase
• Portal venous phase
• Delayed
Understanding the phases
• Liver has dual blood supply
• Normal parenchyma is supplied for 80% by the
portal vein and only for 20% by the hepatic
artery
• All liver tumors get 100% of their blood supply
from the hepatic artery
Arterial phase
• In the arterial phase hypervascular tumors will
enhance via the hepatic artery, when normal
liver parenchyma does not yet enhances,
because contrast is not yet in the portal
venous system.
• Hypervascular tumors will enhance optimally
at 35 sec after contrast injection
Portal venous phase
• To detect hypovascular tumors
• Scanning is at about 75 seconds
LIVER TOMOUR
Delayed Phase
• Begins at about 3-4 minutes after contrast injection
and imaging is best done at 10 minutes
• Valuable for washout of contrast(HCC),retention of
contrast(heamangioma),retention of contrast in
fibrous tissue (capsule of HCC, central scar of FNH)
Classification
• Hemangioma
• Focal nodular
hyperplasia
• Adenoma
• Liver cysts
1. Primary liver cancers
• Hepatocellular carcinoma
• Fibrolamellar carcinoma
• Hepatoblastoma
2. Metastases
Benign Malignant
Benign Liver Lesions
1. Hemangioma
2. Focal nodular hyperplasia
3. Adenoma
4. Cysts
Hemangioma
Clinical Features
• The commonest liver tumor
• 5% of autopsies
• Usually single small
• Well demarcated capsule
• Usually asymptomatic
Hemangioma
Diagnosis and Management
Diagnosis
• US: echogenic spot, well demarcated
• CT: venous enhancement from periphery to center
• MRI: high intensity area
• No need for FNA
Treatment
• No need for treatment
Peripheral nodular enhancement follow
by gradual centripetal enhancement
CT/Hemangioma
Focal Nodular Hyperplasia (FNH)
Clinical Features
• Benign nodule formation of normal liver tissue
• Central stellate scar
• More common in young and middle age
women
• No relation with sex hormones
• Usually asymptomatic
• May cause minimal pain
Focal Nodular Hyperplasia (FNH)
Diagnosis and Management
Diagnosis:
• US: Nodule with varying echogenicity
• CT: Hypervascular mass with central scar
• MRI: iso or hypo intense
• FNA: Normal hepatocytes and Kupffer cells with
central core.
Treatment:
• No treatment necessary
• Pregnancy and hormones OK
Homogeneous
Isoattenuation
Immediate
Intense enhancement
Central scar 2/3
CT/FNH
Hepatic Adenoma
Clinical features
• Benign neoplasm composed of normal
hepatocytes no portal tract, central veins, or
bile ducts
• More common in women
• Associated with contraceptive hormones
• Usually asymptomatic but may have RUQ pain
• May presents with rupture, hemorrhage, or
malignant transformation (very rare)
Hepatic Adenoma
Diagnosis and Management
DX
• US: filling defect
• CT: Diffuse arterial enhancement
• MRI: hypo or hyper intense lesion
• FNA : may be needed
Tx
• Stop hormones
• Observe every 6m for 2 y
• If no regression then surgical excision
HA
Adenoma
Liver Cysts
• May be single or multiple
• May be part of polycystic kidney disease
• Patients often asymptomatic
• No specific management required
• Hydated cyst
Malignant Liver Lesions
Malignant Liver Tumors
1. Hepatocellular carcinoma (HCC)
2. Fibro-lamellar carcinoma of the liver
3. Hepatoblastoma
4. Intrahepatic cholangiocarcinoma
5. Others
HCC: Incidence
• The most common primary liver cancer
• The most common tumor in Saudi men
• Increasing in US and all the world
HCC: Risk Factors
The most important risk factor is cirrhosis from
any cause:
1. Hepatitis B (integrates in DNA)
2. Hepatitis C
3. Alcohol
4. Aflatoxin
5. Other
HCC: Clinical Features
• Wt loss and RUQ pain (most common)
• Asymptomatic
• Worsening of pre-existing chronic liver dis
• Acute liver failure
O/E:
• Signs of cirrhosis
• Hard enlarged RUQ mass
• Liver bruit (rare)
HCC: Metastases
• Rest of the liver
• Portal vein
• Lymph nodes
• Lung
• Bone
• Brain
HCC: Systemic Features
• Hypercalcemia
• Hypoglycemia
• Hyperlipidemia
• Hyperthyroidism
HCC: labs
• Labs of liver cirrhosis
AFP (Alfa feto protein)
• Is an HCC tumor marker
• Values more than 100ng/ml are highly
suggestive of HCC
• Elevation seen in more than 70% of pt
HCC: Diagnosis
• Clinical presentation
• Elevated AFP
• US
• Triphasic CT scan: very early arterial perfusion
• MRI
• Biopsy
US: HCC
CT: Venous Phase
CT: Arterial Phase
Hepatocellular carcinoma, CT of the liver before (a) and 15 sec (b), 45 sec (c) and 90 sec
(d), respectively, following intravenous contrast medium administration
HCC: Prognosis
• Tumor size
• Extrahepatic spread
• Underlying liver disease
• Pt performance status
HCC: Liver Transplantation
• Best available treatment
• Removes tumor and liver
• Only if single tumor less than 5cm or less than
3 tumors less than 3 cm each
• Recurrence rate is low
• Not widely available
HCC: Resection
• Feasible for small tumors with preserved liver
function (no jaundice or portal HTN)
• Recurrence rate is high
HCC: Local Ablation
• For non resectable pt
• For pt with advanced liver cirrhosis
• Alcohol injection
• Radiofrequency ablation
• Temporary measure only
Radio Frequency Ablation
Ethanol Injection
HCC: Chemoembolization
• Inject chemotherapy selectively in hepatic
artery
• Then inject an embolic agent
• Only in pt with early cirrhosis
• No role for systemic chemotherapy
Chemoembolization
Fibro-Lamellar Carcinoma
• Presents in young pt (5-35)
• Not related to cirrhosis
• AFP is normal
• CT shows typical stellate scar with radial septa
showing persistant enhancement
Hepatoblastoma
• most common liver cancer in children
• most commonly diagnosed during a child's first
three years of life
• usually present with an abdominal mass
• Patients with familial adenomatous polyposis
(FAP) are risk factor
• Often elevated AFP
• Treatment : Surgical resection, adjuvant CMT,
and liver transplantation
Secondary Liver Metastases
• The most common site for blood born metastases
• Common primaries : colon, breast, lung, stomach,
pancreases, and melanoma
• Mild cholestatic picture (ALP, LDH) with preserved
liver function
• Dx imaging or FNA
• Treatment depends on the primary cancer
• In some cases resection or chemoembolization is
possible
Pre contrast Arterial Phase Portal venous
phase
Delayed
Hepatocelluar Ca Low attenuation Homogenous
enhancement
Washout of
lesion
Isodense
Adenoma Low attenuation Homogenous
enhancement 85%
Iso or
hypodense
Iso or hypodense
Haemangioma Low attenuation Peripheral puddles Partial Fill in Complete fill in
FNH Iso/Low
attenuation
Homogenous
enhancement
Hypodense Isodense
Metastasis(hypervascular) Low attenuation Homogenous
enhancement
Hypodense
Metastasis Low attenuation Hypodense Hypodense
Cyst Low attenuation No enhancement
Abscess Low attenuation may
have irregular margins
Transient regional
increase enhancement
Ring
enhancement
Multiphasic CT of Liver
Summary
• Hemangioma
• Focal nodular
hyperplasia
• Adenoma
• Liver cysts
1. Primary liver cancers
• Hepatocellular carcinoma
• Fibrolamellar carcinoma
• Hepatoblastoma
2. Metastases
Benign Malignant

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Liver tomour

  • 2. DR.SYED UBAID M.S(KEM MUMBAI) FMAS LAPAROSCOPIC AND GENERAL SURGEON ASSOCIATE PROFESSOR OF SURGERY IIMSR,JALNA
  • 3. WORKUP ALGORYHM FOR LIVER MASS Mass on scan History of prior malignancy No history of prior malignancy
  • 4. History • Symptoms - abdominal pain/ pressure effect,fever,anoraxia,weight loss • Patient characteristics (age, gender, use of OCP, risk factors for chronic liver disease ) • History or findings of extrahepatic malignancy
  • 5. Physical examination and investigation • Sign of chronic liver stigmata or portal hypertention • Lymphadenopathy • CBC with PLT , coagulogram , LFT , hepatitis profile , tumor marker • Ultrasound , CT scan , MRI
  • 6. Find needle biopsy • commonly used to assist in the diagnosis of a variety of liver lesions • Disadventage – Increase risk of bleeding and seeding of neoplastic cells – Some type liver lesion cannot diagnosis such as hepatic adenomas and focal nodular hyperplasia
  • 7. Multiphasic CT For detection of liver lesions • Non enhance CT • Arterial phase • Portal venous phase • Delayed
  • 8. Understanding the phases • Liver has dual blood supply • Normal parenchyma is supplied for 80% by the portal vein and only for 20% by the hepatic artery • All liver tumors get 100% of their blood supply from the hepatic artery
  • 9. Arterial phase • In the arterial phase hypervascular tumors will enhance via the hepatic artery, when normal liver parenchyma does not yet enhances, because contrast is not yet in the portal venous system. • Hypervascular tumors will enhance optimally at 35 sec after contrast injection
  • 10. Portal venous phase • To detect hypovascular tumors • Scanning is at about 75 seconds
  • 11.
  • 13. Delayed Phase • Begins at about 3-4 minutes after contrast injection and imaging is best done at 10 minutes • Valuable for washout of contrast(HCC),retention of contrast(heamangioma),retention of contrast in fibrous tissue (capsule of HCC, central scar of FNH)
  • 14. Classification • Hemangioma • Focal nodular hyperplasia • Adenoma • Liver cysts 1. Primary liver cancers • Hepatocellular carcinoma • Fibrolamellar carcinoma • Hepatoblastoma 2. Metastases Benign Malignant
  • 15. Benign Liver Lesions 1. Hemangioma 2. Focal nodular hyperplasia 3. Adenoma 4. Cysts
  • 16. Hemangioma Clinical Features • The commonest liver tumor • 5% of autopsies • Usually single small • Well demarcated capsule • Usually asymptomatic
  • 17. Hemangioma Diagnosis and Management Diagnosis • US: echogenic spot, well demarcated • CT: venous enhancement from periphery to center • MRI: high intensity area • No need for FNA Treatment • No need for treatment
  • 18. Peripheral nodular enhancement follow by gradual centripetal enhancement
  • 20. Focal Nodular Hyperplasia (FNH) Clinical Features • Benign nodule formation of normal liver tissue • Central stellate scar • More common in young and middle age women • No relation with sex hormones • Usually asymptomatic • May cause minimal pain
  • 21. Focal Nodular Hyperplasia (FNH) Diagnosis and Management Diagnosis: • US: Nodule with varying echogenicity • CT: Hypervascular mass with central scar • MRI: iso or hypo intense • FNA: Normal hepatocytes and Kupffer cells with central core. Treatment: • No treatment necessary • Pregnancy and hormones OK
  • 24. Hepatic Adenoma Clinical features • Benign neoplasm composed of normal hepatocytes no portal tract, central veins, or bile ducts • More common in women • Associated with contraceptive hormones • Usually asymptomatic but may have RUQ pain • May presents with rupture, hemorrhage, or malignant transformation (very rare)
  • 25. Hepatic Adenoma Diagnosis and Management DX • US: filling defect • CT: Diffuse arterial enhancement • MRI: hypo or hyper intense lesion • FNA : may be needed Tx • Stop hormones • Observe every 6m for 2 y • If no regression then surgical excision
  • 26. HA
  • 28. Liver Cysts • May be single or multiple • May be part of polycystic kidney disease • Patients often asymptomatic • No specific management required • Hydated cyst
  • 30. Malignant Liver Tumors 1. Hepatocellular carcinoma (HCC) 2. Fibro-lamellar carcinoma of the liver 3. Hepatoblastoma 4. Intrahepatic cholangiocarcinoma 5. Others
  • 31. HCC: Incidence • The most common primary liver cancer • The most common tumor in Saudi men • Increasing in US and all the world
  • 32. HCC: Risk Factors The most important risk factor is cirrhosis from any cause: 1. Hepatitis B (integrates in DNA) 2. Hepatitis C 3. Alcohol 4. Aflatoxin 5. Other
  • 33. HCC: Clinical Features • Wt loss and RUQ pain (most common) • Asymptomatic • Worsening of pre-existing chronic liver dis • Acute liver failure O/E: • Signs of cirrhosis • Hard enlarged RUQ mass • Liver bruit (rare)
  • 34. HCC: Metastases • Rest of the liver • Portal vein • Lymph nodes • Lung • Bone • Brain
  • 35. HCC: Systemic Features • Hypercalcemia • Hypoglycemia • Hyperlipidemia • Hyperthyroidism
  • 36. HCC: labs • Labs of liver cirrhosis AFP (Alfa feto protein) • Is an HCC tumor marker • Values more than 100ng/ml are highly suggestive of HCC • Elevation seen in more than 70% of pt
  • 37. HCC: Diagnosis • Clinical presentation • Elevated AFP • US • Triphasic CT scan: very early arterial perfusion • MRI • Biopsy
  • 41. Hepatocellular carcinoma, CT of the liver before (a) and 15 sec (b), 45 sec (c) and 90 sec (d), respectively, following intravenous contrast medium administration
  • 42. HCC: Prognosis • Tumor size • Extrahepatic spread • Underlying liver disease • Pt performance status
  • 43. HCC: Liver Transplantation • Best available treatment • Removes tumor and liver • Only if single tumor less than 5cm or less than 3 tumors less than 3 cm each • Recurrence rate is low • Not widely available
  • 44. HCC: Resection • Feasible for small tumors with preserved liver function (no jaundice or portal HTN) • Recurrence rate is high
  • 45. HCC: Local Ablation • For non resectable pt • For pt with advanced liver cirrhosis • Alcohol injection • Radiofrequency ablation • Temporary measure only
  • 48. HCC: Chemoembolization • Inject chemotherapy selectively in hepatic artery • Then inject an embolic agent • Only in pt with early cirrhosis • No role for systemic chemotherapy
  • 50. Fibro-Lamellar Carcinoma • Presents in young pt (5-35) • Not related to cirrhosis • AFP is normal • CT shows typical stellate scar with radial septa showing persistant enhancement
  • 51. Hepatoblastoma • most common liver cancer in children • most commonly diagnosed during a child's first three years of life • usually present with an abdominal mass • Patients with familial adenomatous polyposis (FAP) are risk factor • Often elevated AFP • Treatment : Surgical resection, adjuvant CMT, and liver transplantation
  • 52. Secondary Liver Metastases • The most common site for blood born metastases • Common primaries : colon, breast, lung, stomach, pancreases, and melanoma • Mild cholestatic picture (ALP, LDH) with preserved liver function • Dx imaging or FNA • Treatment depends on the primary cancer • In some cases resection or chemoembolization is possible
  • 53.
  • 54.
  • 55. Pre contrast Arterial Phase Portal venous phase Delayed Hepatocelluar Ca Low attenuation Homogenous enhancement Washout of lesion Isodense Adenoma Low attenuation Homogenous enhancement 85% Iso or hypodense Iso or hypodense Haemangioma Low attenuation Peripheral puddles Partial Fill in Complete fill in FNH Iso/Low attenuation Homogenous enhancement Hypodense Isodense Metastasis(hypervascular) Low attenuation Homogenous enhancement Hypodense Metastasis Low attenuation Hypodense Hypodense Cyst Low attenuation No enhancement Abscess Low attenuation may have irregular margins Transient regional increase enhancement Ring enhancement Multiphasic CT of Liver
  • 56. Summary • Hemangioma • Focal nodular hyperplasia • Adenoma • Liver cysts 1. Primary liver cancers • Hepatocellular carcinoma • Fibrolamellar carcinoma • Hepatoblastoma 2. Metastases Benign Malignant

Editor's Notes

  1. Only a minority of tumors contain calcifications, cystic components, fat or hemorrhage and will be detected on a NECT.
  2. Tumors enhance in arterial phase. Liver will enhance in the portal venous phase
  3. Will be visible as hyperdense lesions in a relatively hypodense liver
  4. also called the hepatic phase because there already must be enhancement of the hepatic veins
  5. HCC Cirrhotic liver with a single nodule in the right lobe showing marked arterial phase enhancement and early wash off in the portovenous phase are diagnostic features of a HCC.